NM_181725.4(METTL2A):c.968A>C (p.Tyr323Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 8, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004359255.1
Allele description [Variation Report for NM_181725.4(METTL2A):c.968A>C (p.Tyr323Ser)]
NM_181725.4(METTL2A):c.968A>C (p.Tyr323Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens uncharacterized LOC105377213 (LOC105377213), long non-coding RNA
Homo sapiens uncharacterized LOC105377213 (LOC105377213), long non-coding RNAgi|1008806563|ref|NR_135614.1|Nucleotide
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Last Updated: Oct 13, 2024